Intrathecal Ziconotide in Chemotherapy Induced Peripheral Neuropathy
Part of paid clinical trials in St Louis, Missouri.
- Sponsor
- Christian Hospital Northeast Northwest
- Study ID
- NCT07499882
- Status
- Not Yet Recruiting
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Conditions
- Chemotherapy Induced Peripheral Neuropathy (CIPN)
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 100 Years
- Healthy Volunteers
- Not accepted
Interventions
- Ziconotide — DRUGReal world evidence trial. Patients that are on intrathecal ziconotide will be observed for two years, to determine whether or not this drug is effective for chemotherapy induced peripheral neuropathy.
Study Details
The purpose of this observational, data collection, research is to evaluate if ziconotide, a commercially approved medication given by a FDA cleared intrathecal pump, for chronic pain is effective in the treatment of chemotherapy-induced peripheral neuropathy (CIPN) a common and often long-lasting side effect of cancer treatment.
Key Dates
- Start date
- May 2, 2026
- Status verified
- Mar 2026
- Primary completion
- May 1, 2028
- Completion
- May 1, 2028
Study Design
- Enrollment
- 24 participants (estimated)
Arms
- Arm: Study groupThis is the only group. All subjects will receive ziconotide via the Medtronic Synchromed intrathecal pump.
Primary Outcome Measure
Assess whether or not patients' pain score from VAS changes when receiving intrathecal ziconotide [ Time Frame: From enrollment to the end of treatment at 24 months ]
Central Contacts
- Maksim Shoykhet, BSN314-653-5228
- Cassandra Wania, BSN314-653-5228
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Christian Hospital | St Louis | Missouri | 63136 | Christopher L Beuer, MD (PRINCIPAL_INVESTIGATOR) |
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